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Autoimmune lymphoproliferative syndrome is accompanied by the following clinical manifestations: thrombocytopenia; hemolytic anemia; lymphatic infiltration of T-lymphocytes (splenomegaly, chronic non-malignant lymphadenopathy). In this disease, there is an increased risk of developing lymphomas, severe attacks of immune cytopenia. The disease is rare.
Establishing the diagnosis of APS is based on the analysis of the anamnesis, clinical symptoms, objective finding and laboratory tests.